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TSPYL1 Antibody(C-term)

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • WB - TSPYL1 Antibody(C-term) AP19691b
    TSPYL1 Antibody (C-term) (Cat. #AP19691b) western blot analysis in A549 cell line lysates (35ug/lane).This demonstrates the TSPYL1 antibody detected the TSPYL1 protein (arrow).
    detail
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB, E
Primary Accession Q9H0U9
Other Accession O88852, NP_003300.1
Reactivity Human
Predicted Mouse
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 49192 Da
Antigen Region 343-372 aa
Additional Information
Gene ID 7259
Other Names Testis-specific Y-encoded-like protein 1, TSPY-like protein 1, TSPYL1, TSPYL
Target/Specificity This TSPYL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 343-372 amino acids from the C-terminal region of human TSPYL1.
Dilution WB~~1:1000
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsTSPYL1 Antibody(C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name TSPYL1
Synonyms TSPYL
Cellular Location Nucleus, nucleolus.
Tissue Location Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
Research Areas
Citations (0)
citation

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Background

The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).

References

Vinci, G., et al. Fertil. Steril. 92(4):1347-1350(2009)
de Andrade, T.G., et al. Blood Cells Mol. Dis. 37(2):82-90(2006)
Wang, A.G., et al. Biochem. Biophys. Res. Commun. 345(3):1022-1032(2006)
Hering, R., et al. Genet. Med. 8(1):55-58(2006)
Puffenberger, E.G., et al. Proc. Natl. Acad. Sci. U.S.A. 101(32):11689-11694(2004)

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$ 182.50
$ 70.00
Cat# AP19691b
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